antacid ultra strength

Generic: calcium carbonate

Labeler: cardinal health 110, llc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name antacid ultra strength
Generic Name calcium carbonate
Labeler cardinal health 110, llc.
Dosage Form TABLET, CHEWABLE
Routes
ORAL
Active Ingredients

calcium carbonate 1000 mg/1

Manufacturer
CARDINAL HEALTH 110, LLC.

Identifiers & Regulatory

Product NDC 70000-0683
Product ID 70000-0683_411d7abc-9cd4-0480-e063-6394a90a8bb8
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2026-12-31
Marketing Start 2024-07-08

Pharmacologic Class

Classes
blood coagulation factor [epc] calcium [cs] cations divalent [cs] increased coagulation factor activity [pe] phosphate binder [epc] phosphate chelating activity [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 700000683
Hyphenated Format 70000-0683

Supplemental Identifiers

RxCUI
308892
UPC
0096295143577
UNII
H0G9379FGK

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name antacid ultra strength (source: ndc)
Generic Name calcium carbonate (source: ndc)
Application Number M001 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1000 mg/1
source: ndc
Packaging
  • 72 TABLET, CHEWABLE in 1 BOTTLE (70000-0683-1)
source: ndc

Packages (1)

70000-0683-1 72 TABLET, CHEWABLE in 1 BOTTLE (70000-0683-1)

Ingredients (1)

calcium carbonate (1000 mg/1)

Linked Drug Pages (1)

ANTACID Ultra Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "411d7abc-9cd4-0480-e063-6394a90a8bb8", "openfda": {"upc": ["0096295143577"], "unii": ["H0G9379FGK"], "rxcui": ["308892"], "spl_set_id": ["d267ca31-09bd-46d3-be08-a259642f1b7f"], "manufacturer_name": ["CARDINAL HEALTH 110, LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "72 TABLET, CHEWABLE in 1 BOTTLE (70000-0683-1)", "package_ndc": "70000-0683-1", "marketing_start_date": "20240708"}], "brand_name": "ANTACID Ultra Strength", "product_id": "70000-0683_411d7abc-9cd4-0480-e063-6394a90a8bb8", "dosage_form": "TABLET, CHEWABLE", "pharm_class": ["Blood Coagulation Factor [EPC]", "Calcium [CS]", "Cations", "Divalent [CS]", "Increased Coagulation Factor Activity [PE]", "Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]"], "product_ndc": "70000-0683", "generic_name": "calcium carbonate", "labeler_name": "CARDINAL HEALTH 110, LLC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ANTACID", "brand_name_suffix": "Ultra Strength", "active_ingredients": [{"name": "CALCIUM CARBONATE", "strength": "1000 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240708", "listing_expiration_date": "20261231"}